Your Health. Your Family. Your Choice.
|History of Changes from the VAERS Wayback Machine|
|Vaccination / Manufacturer||Lot / Dose||Site / Route|
|COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH||UNKNOWN / 1||- / -|
Administered by: Other Purchased by: ??
Symptoms: Death, Malaise, Blood test
Life Threatening? No
Birth Defect? No
Permanent Disability? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Other Medications: FENTANYL
Current Illness: Anemia; Palliative care; Renal failure
Preexisting Conditions: Medical History/Concurrent Conditions: Dehydration
Diagnostic Lab Data: Test Date: 20210126; Test Name: blood check; Result Unstructured Data: Test Result:unknown results; Test Date: 20210201; Test Name: blood check; Result Unstructured Data: Test Result:anemia appeared to be better than expected
CDC 'Split Type': NLPFIZER INC2021163972
Write-up: Death; Unwell; This is a spontaneous report from a contactable physician downloaded from the Agency Regulatory Authority-WEB NL-LRB-00442005, received from Regulatory Authority. A 67-year-old female patient received the first dose of bnt162b2 (COMIRNATY, lot# unknown, 0.3ml), via an unspecified route of administration on 26Jan2021 at 0.3 mL, single for covid-19 immunisation; fentanyl (manufacturer unknown, 25 ug), via an unspecified route of administration from an unspecified date to 25Jan2021 at 12 ug, 1x per 3 days, then from 26Jan2021 and ongoing at 25 ug, 1x per 3 days for pain. Medical history included ongoing anemia, ongoing palliative care, ongoing terminal renal failure and dehydration. The patient had already palliative care and was known with increasing anemia. The patient''s concomitant medications were not reported. At the same day as the day of vaccination (26Jan2021), the fentanyl dosage was increased from 12 to 25 ug per hour and blood check was requested for the anemia. Two days after increasing the dosage of fentanyl and administration of Covid 19 vaccine (28Jan2021), the patient became unwell. From that moment, the palliative care was continued and 6 days after vaccination and increasing dosage of fentanyl on 01Feb2021, once more blood check was requested. Anemia appeared to be better than expected but the patient had a terminal renal failure which was induced by dehydration of an already terminal patient. The patient experienced death in Feb2021. The action taken in response to the events for fentanyl was dose not changed. The patient died in Feb2021. It was not reported if an autopsy was performed. Outcome of unwell was unknown. Reporter''s Comment: On 26Jan2021, the decision was made to increase the fentanyl patch and request a lab check. It was known to have an increasing anemia. On Thursday, 28Jan2021, patient became unwell. From that moment on, the palliative policy was continued and on Monday 01Feb2021 a lab test was done. It showed that the anemia was not too bad, but she had terminal kidney failure. This terminal kidney failure can be caused by dehydration in an already terminal lady. Confounding factors: patient was already palliative and it is unclear if this was precipitated. Diagnostic procedures: it was not thought until the time of death, that vaccination may have played a role. No follow-up attempts are possible, information on batch number cannot be obtained.; Reporter''s Comments: From that moment on, the palliative policy was continued and on Monday 01Feb2021 a lab test was done. It showed that the anemia was not too bad, but she had terminal kidney failure. This terminal kidney failure can be caused by dehydration in an already terminal lady. Confounding factors: patient was already palliative and it is unclear if this was precipitated. Diagnostic procedures: it was not thought until the time of death, that vaccination may have played a role.; Reported Cause(s) of Death: Death
Copyright © 2021 National Vaccine Information Center. All rights reserved.
21525 Ridgetop Circle, Suite 100, Sterling, VA 20166